Cook D I, Day M L, Champion M P, Young J A
Department of Physiology, University of Sydney, NSW, Australia.
Pflugers Arch. 1988 Nov;413(1):67-76. doi: 10.1007/BF00581230.
We have performed whole-cell patch-clamp studies on dispersed secretory cells of the rat mandibular gland to determine how beta-adrenergic stimulation causes fluid secretion. When the pipette contained a high K+ solution, the resting membrane potential averaged -33 mV +/- 1.1 (SEM, n = 34) and the clamped cell showed strong outward rectification. We monitored K+ and Cl- currents for periods of 15 min by recording the currents needed to clamp the cell potential at 0 and -80 mV, respectively. Isoproterenol (1-2 mumol/l) caused increases in the clamp current at 0 mV (the K+ current) and at -80 mV (the Cl- current) in about 80% of cases, although the responses were variable in size and time-course; the responses were indistinguishable from those induced by acetylcholine or the Ca2+ ionophore, A23187. The alpha-adrenergic antagonist, phentolamine (1-2 mumol/l), had no effect on the response, but the beta-adrenergic antagonist, propranolol (10 mumol/l), blocked it completely. The isoproterenol response could not be mimicked by application to either surface of the cell membrane, of cyclic AMP (100 mumol/l), forskolin (1 or 20 mumol/l) or cholera toxin (2.5 micrograms/ml). However, increasing the Ca2+-chelating capacity of the pipette solution by raising its EGTA concentration from the customary 0.5 to 20 mmol/l, blocked the response to isoproterenol, suggesting that beta-adrenergic agonists activate Cl- and K+ channels by raising cytosolic Ca2+. Since neomycin, which blocks phospholipase C, blocked the action of isoproterenol without impairing the cell responsiveness to A23187, it appears that isoproterenol, like muscarinic agonists, increased cytosolic Ca2+ via the phosphatidylinositol cycle.
我们对大鼠下颌下腺的分散分泌细胞进行了全细胞膜片钳研究,以确定β-肾上腺素能刺激如何引起液体分泌。当移液管中含有高钾溶液时,静息膜电位平均为-33 mV±1.1(标准误,n = 34),钳制的细胞表现出强烈的外向整流。我们通过分别记录将细胞电位钳制在0和-80 mV所需的电流,监测钾离子和氯离子电流15分钟。异丙肾上腺素(1-2 μmol/L)在约80%的情况下导致0 mV(钾离子电流)和-80 mV(氯离子电流)处的钳制电流增加,尽管反应的大小和时间进程各不相同;这些反应与乙酰胆碱或钙离子载体A23187诱导的反应无法区分。α-肾上腺素能拮抗剂酚妥拉明(1-2 μmol/L)对反应无影响,但β-肾上腺素能拮抗剂普萘洛尔(10 μmol/L)完全阻断了反应。将环磷酸腺苷(100 μmol/L)。福斯可林(1或20 μmol/L)或霍乱毒素(2.5 μg/ml)应用于细胞膜的任何一个表面,都无法模拟异丙肾上腺素的反应。然而,通过将移液管溶液的乙二醇双四乙酸(EGTA)浓度从通常的0.5 mmol/L提高到20 mmol/L来增加其钙离子螯合能力,可阻断对异丙肾上腺素的反应,这表明β-肾上腺素能激动剂通过提高胞质钙离子浓度来激活氯离子和钾离子通道。由于阻断磷脂酶C的新霉素可阻断异丙肾上腺素的作用,而不损害细胞对A23187的反应性,因此似乎异丙肾上腺素与毒蕈碱激动剂一样,通过磷脂酰肌醇循环增加胞质钙离子浓度。